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LUMINEB I

Page Type
Cleared 510(K)
510(k) Number
K884722
510(k) Type
Traditional
Applicant
LUMISCOPE CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1989
Days to Decision
85 days

LUMINEB I

Page Type
Cleared 510(K)
510(k) Number
K884722
510(k) Type
Traditional
Applicant
LUMISCOPE CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1989
Days to Decision
85 days